Digitalis purpurea

UNIISPLATC C01AA03

Last synced from FDA National Drug Code directory (United States) on June 3, 2026

Identification

ManufacturerBoiron

CountryUS (United States)

ATC codeC01AA03

Dispensing—

ReimbursedNo

SourceFDA National Drug Code directory (United States)

Last synced6/3/2026

Packs · 1

ndc11
0220175741
30 [hp_C] in 1 TUBE (0220-1757-41)

Annotations

UNII (FDA Substance ID)

F1T8QT9U8B

DIGITALIS

RxCUI 91235

DailyMed SPL labels

1 version tracked

Raw payload (JSON)

{
  "unii": {
    "unii": "F1T8QT9U8B",
    "rxcui": "91235",
    "inchikey": null,
    "display_name": "DIGITALIS",
    "substance_type": "structurallyDiverse",
    "ingredient_type": "INGREDIENT SUBSTANCE"
  },
  "route": "ORAL",
  "spl_meta": {
    "19ba912f-cd86-4cca-e063-6294a90a233b": {
      "match": "brand_token",
      "title": "DIGITALIS PUR LIQUID [RXHOMEO PRIVATE LIMITED D.B.A. RXHOMEO, INC]",
      "spl_version": "1",
      "published_date": "2024-06-03"
    }
  },
  "productid": "0220-1757_0a0c91f9-28b0-3d6d-e063-6294a90aec12",
  "productndc": "0220-1757",
  "dosage_form": "PELLET",
  "dea_schedule": null,
  "product_type": "HUMAN PRESCRIPTION DRUG",
  "substance_name": "DIGITALIS",
  "proprietary_name": "Digitalis purpurea",
  "active_ingred_unit": "[hp_C]/30[hp_C]",
  "application_number": null,
  "marketing_category": "UNAPPROVED HOMEOPATHIC",
  "nonproprietary_name": "DIGITALIS",
  "start_marketing_date": "19830303",
  "active_numerator_strength": "30"
}

Related drugs

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